EP0758787A1 - Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor made therewith - Google Patents

Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor made therewith Download PDF

Info

Publication number
EP0758787A1
EP0758787A1 EP96904278A EP96904278A EP0758787A1 EP 0758787 A1 EP0758787 A1 EP 0758787A1 EP 96904278 A EP96904278 A EP 96904278A EP 96904278 A EP96904278 A EP 96904278A EP 0758787 A1 EP0758787 A1 EP 0758787A1
Authority
EP
European Patent Office
Prior art keywords
electrolytic capacitor
electrolyte
polyethylene glycol
formulas
driving
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP96904278A
Other languages
German (de)
French (fr)
Other versions
EP0758787A4 (en
EP0758787B1 (en
Inventor
Nario Niibo
Naoko Yoshida
Yoshinori Takamuku
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Publication of EP0758787A1 publication Critical patent/EP0758787A1/en
Publication of EP0758787A4 publication Critical patent/EP0758787A4/en
Application granted granted Critical
Publication of EP0758787B1 publication Critical patent/EP0758787B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/004Details
    • H01G9/02Diaphragms; Separators
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/004Details
    • H01G9/022Electrolytes; Absorbents

Definitions

  • the present invention relates to an electrolyte for driving electrolytic capacitor used in an aluminum electrolytic capacitor, and an electrolytic capacitor using the same.
  • an electrolyte for driving an electrolytic capacitor used in an aluminum electrolytic capacitor is known to be an electrolyte for driving electrolytic capacitor using an organic compound such as gamma-butyrolactone or ethylene glycol as main solvent in which solutes are dissolved, such as boric acid, other inorganic acid, adipic acid, azelaic acid, butyl octane diacid (Japanese Patent Publication 60-13293), 5,6-decane dicarboxylic acid (Japanese Patent Publication 63-15738), dibasic acid having side chain (Japanese Laid-open Patent 1-45539), other dibasic acid, and their salts.
  • an organic compound such as gamma-butyrolactone or ethylene glycol
  • solutes such as boric acid, other inorganic acid, adipic acid, azelaic acid, butyl octane diacid
  • Japanese Patent Publication 60-13293 Japanese Patent Publication 60
  • Such compounds have the advantage of increasing the effect of heightening the spark generation voltage as the amount of addition and molecular weight are larger, but solubility in organic solvent, especially at low temperature, is lowered, and precipitation occurs, there arises a limit for selection of amount of addition and molecular weight. It is better to use these compounds at molecular weight of 1000 or less for the sake of precipitation at low temperature. In such range of molecular weight, however, it is not enough to raise the spark generation voltage, and there is a contradictory problem of inducing short puncture at the time of product aging.
  • precipitation at low temperature may be prevented by adding sufficient water to the electrolyte for driving electrolytic capacitor.
  • the electrolyte for driving electrolytic capacitor with sufficient addition of water the vapor pressure in the aluminum electrolytic capacitor is raised due to the effect of water, and it is hard to use at 100°C or higher temperature.
  • the invention is intended to solve the problems of the prior art, and it is hence a primary object thereof to present an electrolyte for driving electrolytic capacitor capable of sufficiently heightening the spark generation voltage and chemical conversion character of formed oxidation film, not precipitating even at low temperature, and an electrolytic capacitor using the same.
  • Fig. 1 is a characteristic diagram showing chemical conversion factor of formed oxide film of an electrolyte for driving electrolytic capacitor in an embodiment of the invention and an electrolyte for driving electrolytic capacitor in prior art
  • Fig. 2 is a perspective view showing an element portion of an aluminum electrolytic capacitor.
  • the invention relates to an electrolyte for driving electrolytic capacitor prepared by using a solvent mainly composed of organic compound, and dissolving one or more solutes selected from the group consisting of inorganic acids and organic acids, more specifically adding and dissolving at least one of copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2), or both of the copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) simultaneously, and an electrolytic capacitor using the same.
  • compositions of the electrolyte for driving electrolytic capacitor and characteristics of embodiments 1 to 20 of the invention and prior arts 1 to 7 are summarized in Table 2, Table 3, and Table 4.
  • Table 2 Table 3
  • Table 4 Table 4
  • the characteristic diagram showing the chemical conversion factor of formed oxidation film of prior arts 6 and 7 and embodiment 20 of the invention are given in Fig. 1.
  • the water content in the electrolyte for driving electrolytic capacitor was commonly adjusted at 1.5% in embodiments 1 to 20 of the invention and prior arts 1 to 7.
  • the spark generation voltage can be raised while maintaining the conductivity, so that the dielectric strength can be stabilized without raising the resistance of the aluminum electrolytic capacitor.
  • Table 5 shows results of life test of aluminum electrolytic capacitors by preparing 20 samples each of aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in prior arts 2 and 3 and aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in embodiments 2, 3 and 4 shown in Table 2 and Table 3.
  • the rating of all aluminum electrolytic capacitors was 250 WV 670 ⁇ F, and the test temperature was 110°C.
  • Fig. 2 shows the composition of the element portion of the aluminum electrolytic capacitor, and as shown in Fig. 2, the element is composed by taking up an anode foil 1 as a positive electrode made of aluminum, and a cathode foil 2 as negative electrode made of also aluminum oppositely through an interposed separator 3. An outgoing lead 4 is connected to the anode foil 1 and cathode foil 2 of this element.
  • Table 6 shows results of life test of aluminum electrolytic capacitors, by preparing 20 samples each of aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in prior art 6 and aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in embodiment 20 shown in Table 2 and Table 4.
  • the rating of all aluminum electrolytic capacitors was 450 WV 330 ⁇ F, and the test temperature was 110°C.
  • the solvent of these embodiments of the invention described so far is ethylene glycol, but it was confirmed that similar effects were obtained by selecting, instead, at least one type of glycol ethers such as ethylene glycol monomethyl ether, acid amids such as dimethyl formamide, and cyclic esters such as gamma-butyrolactone.
  • glycol ethers such as ethylene glycol monomethyl ether, acid amids such as dimethyl formamide, and cyclic esters such as gamma-butyrolactone.
  • Table 7 shows embodiment 21 of the invention using gamma-butyrolactone as solvent and prior art 8 as comparative example.
  • the spark generation voltage can be sufficiently heightened.
  • the structure of the copolymer of polyethylene glycol and polypropylene glycol is similar in performance whether in block copolymer or in random copolymer, and similar effects are expected.
  • At least one or more of copolymers of polyethylene glycol and polypropylene glycol, or both of copolymers of polyethylene glycol and polypropylene glycols shown in formulas (1) and (2) may be added and dissolved simultaneously.
  • the molecular weight of the copolymer of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) is preferably in a range of 1000 to 20000 as clear from the embodiments of the invention, and the amount of addition of the copolymer of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) is preferably in a range of 0.1 to 10 wt.% as clear from the embodiments of the invention.
  • the copolymer used in the electrolyte for driving the electrolytic capacitor of the invention is prepared by copolymerizing polyethylene glycol of which defect is high crystallinity, and polypropylene glycol low in solubility in organic solvent but low in degree of crystallization, mutual defects are compensated for each other, so that the problem of precipitation at low temperature can be solved.
  • the range of selection of usable amount of addition and molecular weight is broadened, and the spark generation voltage and chemical conversion factor of formed oxidation film can be enhanced, so that the reliability of the aluminum electrolytic capacitor from low voltage to medium and high voltage can be enhanced.

Abstract

The invention relates to an electrolyte for driving electrolytic capacitor and an electrolytic capacitor using the same, and by preparing by using a solvent mainly composed of organic compound, and dissolving one or more solutes selected from the group consisting of inorganic acids and organic acids, more specifically adding and dissolving at least one of copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2), or both of the copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) simultaneously, the spark generation voltage and chemical conversion factor of formed oxidation film are enhanced, thereby improving the reliability of the electrolytic capacitor.

        HO - (C2H4O)n - (C3H6O)m - (C2H4O)n - H     (1)

(n and m are arbitrary natural numbers.)

        HO - [(C2H4O)n - (C3H6O)m]l - H     (2)

(n, m, and l are arbitrary natural numbers.)

Description

    TECHNICAL FIELD
  • The present invention relates to an electrolyte for driving electrolytic capacitor used in an aluminum electrolytic capacitor, and an electrolytic capacitor using the same.
  • BACKGROUND ART
  • Generally, an electrolyte for driving an electrolytic capacitor used in an aluminum electrolytic capacitor is known to be an electrolyte for driving electrolytic capacitor using an organic compound such as gamma-butyrolactone or ethylene glycol as main solvent in which solutes are dissolved, such as boric acid, other inorganic acid, adipic acid, azelaic acid, butyl octane diacid (Japanese Patent Publication 60-13293), 5,6-decane dicarboxylic acid (Japanese Patent Publication 63-15738), dibasic acid having side chain (Japanese Laid-open Patent 1-45539), other dibasic acid, and their salts.
  • In such electrolytes for driving electrolytic capacitor, since the spark generation voltage and chemical conversion factor are not enough, and when used in an electrolytic capacitor, it may cause troubles such as short puncture due to aging. It has been therefore attempted to solve the problems by adding polyethylene glycol (Japanese Patent Publication 3-76776) or polyglycerin (Japanese Laid-open Patent 2-194611), thereby enhancing the spark generation voltage.
  • Such compounds have the advantage of increasing the effect of heightening the spark generation voltage as the amount of addition and molecular weight are larger, but solubility in organic solvent, especially at low temperature, is lowered, and precipitation occurs, there arises a limit for selection of amount of addition and molecular weight. It is better to use these compounds at molecular weight of 1000 or less for the sake of precipitation at low temperature. In such range of molecular weight, however, it is not enough to raise the spark generation voltage, and there is a contradictory problem of inducing short puncture at the time of product aging.
  • Or, when such compounds are composed so as to increase in the amount of addition and molecular weight, precipitation at low temperature may be prevented by adding sufficient water to the electrolyte for driving electrolytic capacitor. In the electrolyte for driving electrolytic capacitor with sufficient addition of water, however, the vapor pressure in the aluminum electrolytic capacitor is raised due to the effect of water, and it is hard to use at 100°C or higher temperature.
  • These compounds are more likely to crystallize as the molecular weight increases, and if solidified in wax form, it causes a serious difficulty in working efficiency in mass production.
  • DISCLOSURE OF THE INVENTION
  • The invention is intended to solve the problems of the prior art, and it is hence a primary object thereof to present an electrolyte for driving electrolytic capacitor capable of sufficiently heightening the spark generation voltage and chemical conversion character of formed oxidation film, not precipitating even at low temperature, and an electrolytic capacitor using the same.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • Fig. 1 is a characteristic diagram showing chemical conversion factor of formed oxide film of an electrolyte for driving electrolytic capacitor in an embodiment of the invention and an electrolyte for driving electrolytic capacitor in prior art, and Fig. 2 is a perspective view showing an element portion of an aluminum electrolytic capacitor.
  • BEST MODES OF CARRYING OUT THE INVENTION
  • The invention relates to an electrolyte for driving electrolytic capacitor prepared by using a solvent mainly composed of organic compound, and dissolving one or more solutes selected from the group consisting of inorganic acids and organic acids, more specifically adding and dissolving at least one of copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2), or both of the copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) simultaneously, and an electrolytic capacitor using the same.

            HO - (C2H4O)n - (C3H6O)m - (C2H4O)n - H     (1)

    (n and m are arbitrary natural numbers.)

            HO - [(C2H4O)n - (C3H6O)m]l - H     (2)

    (n, m, and l are arbitrary natural numbers.)
  • Embodiments of the invention are described below. First, concerning precipitation at low temperature, results of measurements of an embodiment of the invention and prior art are shown in Table 1. Table 1
    Composition After 3 hrs at -15°C
    Prior art Ethylene glycol 85
    Polyethylene glycol #4000 10 Precipitated
    Ammonium adipate 5
    Embodiment Ethylene glycol 85
    Polyethylene glycol: polypropylene glycol =5 : 5 #4000 10 Not precipitated
    Ammonium adipate 5
  • As clear from Table 1, in the electrolyte for driving electrolytic capacitor in the embodiment of the invention, no precipitation was observed after 3 hours at -15°C. Only an example of using adipic acid is shown in Table 1, but when other organic acids or inorganic acids were used, same results as in the embodiment of the invention were obtained. Therefore, the low temperature precipitation property of the invention is known to be excellent regardless of the type of the selected solutes.
  • Compositions of the electrolyte for driving electrolytic capacitor and characteristics of embodiments 1 to 20 of the invention and prior arts 1 to 7 are summarized in Table 2, Table 3, and Table 4. Incidentally, the characteristic diagram showing the chemical conversion factor of formed oxidation film of prior arts 6 and 7 and embodiment 20 of the invention are given in Fig. 1. The water content in the electrolyte for driving electrolytic capacitor was commonly adjusted at 1.5% in embodiments 1 to 20 of the invention and prior arts 1 to 7. Table 2
    Composition (wt%) Conductivity (mS/cm) Spark generation voltage (V)
    Prior art 1 Ethylene glycol 85 0.5 550
    Ammonium borate 15
    Prior art 2 Ethylene glycol 90 2.8 320
    Diammonium azelate 10
    Prior art 3 Ethylene glycol 90 3.2 280
    Ammonium benzoate 10
    Prior art 4 Ethylene glycol 90 3.5 300
    Diammonium adipate 10
    Prior art 5 Ethylene glycol 90
    5,6-Decane dicarboxylic acid diammonium 10 2.0 420
    Prior art 6 Ethylene glycol 90
    1,7-Octane dicarboxylic acid diammonium 10 2.0 420
    Prior art 7 Ethylene glycol 80
    Polyglycerin #1000 10 1.5 460
    1,7-Octane dicarboxylic acid diammonium 10
    Figure imgb0001
    Figure imgb0002
    Figure imgb0003
    Figure imgb0004
  • As clear from Table 2, Table 3 and Table 4, in the embodiments of the invention, when the solutes are same as in the prior arts, the spark generation voltage can be enhanced notably. As a result, the incidence of short puncture in aging process can be lowered. Still more, the electrolyte for driving electrolytic capacitor adding copolymers of polyethylene glycol and polypropylene glycol of the invention can dramatically enhance the chemical conversion factor of the formed oxidation film, as well as the spark generation voltage, as understood from Fig. 1.
  • Moreover, as known from embodiments 18 to 20 of the invention in Table 2, by adjusting the amount of addition, the spark generation voltage can be raised while maintaining the conductivity, so that the dielectric strength can be stabilized without raising the resistance of the aluminum electrolytic capacitor.
  • Table 5 shows results of life test of aluminum electrolytic capacitors by preparing 20 samples each of aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in prior arts 2 and 3 and aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in embodiments 2, 3 and 4 shown in Table 2 and Table 3. The rating of all aluminum electrolytic capacitors was 250 WV 670 µF, and the test temperature was 110°C.
  • Fig. 2 shows the composition of the element portion of the aluminum electrolytic capacitor, and as shown in Fig. 2, the element is composed by taking up an anode foil 1 as a positive electrode made of aluminum, and a cathode foil 2 as negative electrode made of also aluminum oppositely through an interposed separator 3. An outgoing lead 4 is connected to the anode foil 1 and cathode foil 2 of this element.
  • The element in such composition is impregnated with a driving electrolyte, and the element is sealed in a case such as an aluminum case, so that an aluminum electrolytic capacitor is composed. Table 5
    Initial characteristic After 2000 hrs at 110°C Remarks
    tan δ (%) LC(µA) ΔC% tan δ (%) LC(µA)
    Prior art 2 6.0 32.5 -6.8 15.0 43.2 Open valve trouble in 3/20 samples
    Prior art 3 5.1 65.3 Test discontinued Short puncture in 15/20 samples
    Embodiment
    2 5.7 21.5 0 6.5 10.1 No problem
    Embodiment
    3 5.7 25.1 0 6.5 9.7 No problem
    Embodiment
    4 5.7 20.3 0 6.5 9.5 No problem
  • As clear from Table 5, in the aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in prior art 2, open valve troubles occurred in 3 out of 20 samples during life test. In prior art 3, short puncture occurring in 15 out of 20 samples during aging, and the life test could not be continued. By contrast, in the aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in embodiments 2, 3 and 4 of the invention, short puncture did not occur during aging or throughout the life test, and the characteristics in 2000 hours at 110°C of life test, as compared with the initial characteristics, were small in change rate of electrostatic capacity (ΔC), small in increase of tangent of loss angle ( tan δ
    Figure imgb0005
    ), and stable in leakage current (LC), so that aluminum electrolytic capacitors of stable life characteristics could be obtained.
  • Moreover, results of evaluation in 450 WV class are shown in Table 6. Table 6 shows results of life test of aluminum electrolytic capacitors, by preparing 20 samples each of aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in prior art 6 and aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in embodiment 20 shown in Table 2 and Table 4. The rating of all aluminum electrolytic capacitors was 450 WV 330 µF, and the test temperature was 110°C. Table 6
    Initial characteristic After 2000 hrs at 110°C Remarks
    tan δ (%) LC(µA) ΔC% tan δ (%) LC(µA)
    Prior art 6 3.1 28.4 Test discontinued Short puncture in 10/20 samples
    Embodiment
    20 3.8 20.5 0 5.1 9.5 No problem
  • As clear from Table 6, in the aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in prior art 6, short puncture occurring in 10 out of 20 samples during aging. By contrast, in the aluminum electrolytic capacitors using the electrolyte for driving electrolytic capacitor in embodiment 20 of the invention, short puncture did not occur during aging or throughout the life test, and the characteristics in 2000 hours at 110°C of life test, as compared with the initial characteristics, were small in change rate of electrostatic capacity (ΔC), small in increase of tangent of loss angle ( tan δ
    Figure imgb0006
    ), and stable in leakage current (LC), so that aluminum electrolytic capacitors of stable life characteristics could be obtained.
  • The solvent of these embodiments of the invention described so far is ethylene glycol, but it was confirmed that similar effects were obtained by selecting, instead, at least one type of glycol ethers such as ethylene glycol monomethyl ether, acid amids such as dimethyl formamide, and cyclic esters such as gamma-butyrolactone. As an example, Table 7 shows embodiment 21 of the invention using gamma-butyrolactone as solvent and prior art 8 as comparative example. Table 7
    Composition (wt%) Conductivity (mS/cm) Spark generation voltage (V)
    Prior art 8 Gamma-butyrolactone 80
    Phthalic acid 10 3.50 100
    Triethylamine 3
    Embodiment 21 Ethylene glycol 80
    Polyethylene glycol: polypropylene glycol = 5:5 #2000 2 3.50 150
    Phthalic acid 10
    Triethylamine 3
  • As clear from Table 7, even in a different solvent system, the spark generation voltage can be sufficiently heightened.
  • Incidentally, as shown in formulas (1) and (2), the structure of the copolymer of polyethylene glycol and polypropylene glycol is similar in performance whether in block copolymer or in random copolymer, and similar effects are expected.
  • When adding and dissolving the copolymer of polyethylene glycol and polypropylene glycol in formulas (1) and (2) in an electrolyte for driving electrolytic capacitor, at least one or more of copolymers of polyethylene glycol and polypropylene glycol, or both of copolymers of polyethylene glycol and polypropylene glycols shown in formulas (1) and (2) may be added and dissolved simultaneously.
  • The molecular weight of the copolymer of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) is preferably in a range of 1000 to 20000 as clear from the embodiments of the invention, and the amount of addition of the copolymer of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) is preferably in a range of 0.1 to 10 wt.% as clear from the embodiments of the invention.
  • INDUSTRIAL APPLICABILITY
  • As obvious from the description herein, since the copolymer used in the electrolyte for driving the electrolytic capacitor of the invention is prepared by copolymerizing polyethylene glycol of which defect is high crystallinity, and polypropylene glycol low in solubility in organic solvent but low in degree of crystallization, mutual defects are compensated for each other, so that the problem of precipitation at low temperature can be solved. By solving this problem, the range of selection of usable amount of addition and molecular weight is broadened, and the spark generation voltage and chemical conversion factor of formed oxidation film can be enhanced, so that the reliability of the aluminum electrolytic capacitor from low voltage to medium and high voltage can be enhanced.

Claims (4)

  1. An electrolyte for driving electrolytic capacitor prepared by using a solvent mainly composed of organic compound, and dissolving one or more solutes selected from the group consisting of inorganic acids and organic acids, more specifically adding and dissolving at least one of copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2), or both of the copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) simultaneously.

            HO - (C2H4O)n - (C3H6O)m - (C2H4O)n - H     (1)

    (n and m are arbitrary natural numbers.)

            HO - [(C2H4O)n - (C3H6O)m]l -H     (2)

    (n, m, and l are arbitrary natural numbers.)
  2. An electrolyte for driving electrolytic capacitor of claim 1, wherein the molecular weight of the copolymer of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) ranges from 1000 to 20000.
  3. An electrolyte for driving electrolytic capacitor of claim 1, wherein the amount of addition of the copolymer of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) ranges from 0.1 to 10 wt.%.
  4. An electrolytic capacitor using an electrolyte for driving electrolytic capacitor prepared by using a solvent mainly composed of organic compound, and dissolving one or more solutes selected from the group consisting of inorganic acids and organic acids, more specifically adding and dissolving at least one of copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2), or both of the copolymers of polyethylene glycol and polypropylene glycol shown in formulas (1) and (2) simultaneously.

            HO - (C2H4O)n - (C3H6O)m - (C2H4O)n - H     (1)

    (n and m are arbitrary natural numbers.)

            HO - [(C2H4O)n - (C3H6O)m]l - H     (2)

    (n, m, and l are arbitrary natural numbers. )
EP96904278A 1995-03-02 1996-02-29 Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor made therewith Expired - Lifetime EP0758787B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP42892/95 1995-03-02
JP04289295A JP3538251B2 (en) 1995-03-02 1995-03-02 Electrolyte for driving electrolytic capacitors
PCT/JP1996/000473 WO1996027201A1 (en) 1995-03-02 1996-02-29 Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor made therewith

Publications (3)

Publication Number Publication Date
EP0758787A1 true EP0758787A1 (en) 1997-02-19
EP0758787A4 EP0758787A4 (en) 2005-10-12
EP0758787B1 EP0758787B1 (en) 2006-10-11

Family

ID=12648692

Family Applications (1)

Application Number Title Priority Date Filing Date
EP96904278A Expired - Lifetime EP0758787B1 (en) 1995-03-02 1996-02-29 Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor made therewith

Country Status (7)

Country Link
US (1) US5776358A (en)
EP (1) EP0758787B1 (en)
JP (1) JP3538251B2 (en)
KR (1) KR100304163B1 (en)
CN (1) CN1134801C (en)
DE (1) DE69636615T2 (en)
WO (1) WO1996027201A1 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3551035B2 (en) * 1998-08-31 2004-08-04 松下電器産業株式会社 Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor using the same
JP2004311482A (en) * 2003-04-02 2004-11-04 Sanyo Chem Ind Ltd Electrolytic solution for electrolytic capacitor
JP4379156B2 (en) 2004-03-03 2009-12-09 パナソニック株式会社 Aluminum electrolytic capacitor
JP5810292B2 (en) * 2010-02-15 2015-11-11 パナソニックIpマネジメント株式会社 Electrolytic capacitor
JP6442162B2 (en) * 2014-05-22 2018-12-19 サン電子工業株式会社 Electrolytic capacitor
CN108666616A (en) * 2017-03-31 2018-10-16 比亚迪股份有限公司 A kind of lithium-ion battery electrolytes and battery

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02312218A (en) * 1989-05-26 1990-12-27 Nichicon Corp Electrolyte for driving of electrolytic capacitor
JPH0374827A (en) * 1989-08-16 1991-03-29 Matsushita Electric Ind Co Ltd Electrolyte for driving electrolytic capacitor
EP0591810A1 (en) * 1992-09-29 1994-04-13 Matsushita Electric Industrial Co., Ltd. Electrolyte for use in an electrolytic capacitor and the electrolytic capacitor

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69016239T2 (en) * 1989-04-04 1995-05-24 Matsushita Electric Ind Co Ltd Electrolyte for electrolytic capacitors and capacitor containing them.

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02312218A (en) * 1989-05-26 1990-12-27 Nichicon Corp Electrolyte for driving of electrolytic capacitor
JPH0374827A (en) * 1989-08-16 1991-03-29 Matsushita Electric Ind Co Ltd Electrolyte for driving electrolytic capacitor
EP0591810A1 (en) * 1992-09-29 1994-04-13 Matsushita Electric Industrial Co., Ltd. Electrolyte for use in an electrolytic capacitor and the electrolytic capacitor

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 015, no. 106 (E-1044), 13 March 1991 (1991-03-13) -& JP 02 312218 A (NICHICON CORP), 27 December 1990 (1990-12-27) *
PATENT ABSTRACTS OF JAPAN vol. 015, no. 240 (E-1079), 20 June 1991 (1991-06-20) -& JP 03 074827 A (MATSUSHITA ELECTRIC IND CO LTD), 29 March 1991 (1991-03-29) *
See also references of WO9627201A1 *

Also Published As

Publication number Publication date
KR970703037A (en) 1997-06-10
EP0758787A4 (en) 2005-10-12
CN1148442A (en) 1997-04-23
CN1134801C (en) 2004-01-14
JPH08241831A (en) 1996-09-17
DE69636615T2 (en) 2007-01-18
EP0758787B1 (en) 2006-10-11
KR100304163B1 (en) 2001-11-22
JP3538251B2 (en) 2004-06-14
WO1996027201A1 (en) 1996-09-06
DE69636615D1 (en) 2006-11-23
US5776358A (en) 1998-07-07

Similar Documents

Publication Publication Date Title
US7411777B2 (en) Electrolytic solution for electric double layer capacitor and electric double layer capacitor
US6288889B1 (en) Electrolytic solution for electrolytic capacitor and electrolytic capacitor using the same
US7004983B2 (en) Polymer electrolyte composite for driving an electrolytic capacitor, an electrolytic capacitor using the same, and a method of making the electrolytic capacitor
KR100402997B1 (en) Polymer Solid Electrolyte
EP1724795A1 (en) Electrolytic solution for electric double layer capacitor and electric double layer capacitor
EP0758787A1 (en) Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor made therewith
EP0591810B1 (en) Electrolyte for use in an electrolytic capacitor and the electrolytic capacitor
EP2555213B1 (en) Electrolyte for electrolytic capacitor
KR20150065689A (en) Electrolytic solution for electrolytic capacitor, and electrolytic capacitor
US20040214078A1 (en) Electrochemical cell
KR100328262B1 (en) A method for preparing electrolytes for aluminum electrolysis condensor for high voltage and the electrolyte prepared therefrom
JPH06208934A (en) Electrolyte for driving electrolytic capacitor
JP3473288B2 (en) Electrolytic solution for driving electrolytic capacitor and electrolytic capacitor using the same
KR20030034977A (en) Electrolyte for aluminium electrolysis condenser of low voltage and electrolysis condenser having the same
JPH10106892A (en) Electrolyte solution for driving electrolytic capacitor and electrolytic capacitor using the same
KR100348923B1 (en) electrolyte for driving electrolytic condenser and electrolytic condenser using the same
JP2701876B2 (en) Electrolyte for electrolytic capacitors
JP2003249421A (en) Polymer electrolytic complex for electrolytic-capacitor driving, electrolytic capacitor using the same, and manufacturing method of the same
JP3991592B2 (en) Electrolytic solution for electrolytic capacitor driving and electrolytic capacitor using the same
JP3684856B2 (en) Electrolytic solution for electrolytic capacitor driving and electrolytic capacitor using the same
JPH0522374B2 (en)
CN112837940A (en) Conductive polymer mixed electrolytic capacitor
JPH05159978A (en) Electrolyte solution for electrolytic-capacitor
JPH0810663B2 (en) Electrolytic solution for electrolytic capacitors
JPH11186108A (en) Aluminum electrolytic capacitor and electrolytic solution for driving it

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE FR GB

17P Request for examination filed

Effective date: 19970212

A4 Supplementary search report drawn up and despatched

Effective date: 20050830

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REF Corresponds to:

Ref document number: 69636615

Country of ref document: DE

Date of ref document: 20061123

Kind code of ref document: P

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20070214

Year of fee payment: 12

ET Fr: translation filed
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20070712

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20070209

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20080221

Year of fee payment: 13

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20080229

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20081031

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20080229

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20080229

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090901